Hyperpigmentation, Familial Progressive, 1 (FPH1)

Alias:
Fph1
Fph
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperpigmentation, Familial Progressive, 1, also known as fph1, is related to hyperpigmentation with or without hypopigmentation, familial progressive and hypomagnesemia 2, renal. An important gene associated with Hyperpigmentation, Familial Progressive, 1 is HPP1 (Hyperpigmentation, Progressive, 1). Affiliated tissues include skin, and related phenotype is hyperpigmentation of the skin.

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
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